| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06822 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:12964260-12965600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:12964732-12964750 | AGAAGGAGGGAAGAAAGG | + | 6.75 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I012824 | chr2 | 12964201 | 12965530 |
|
Enhancer Sequence | AGGAGTGTGT GAGCATCCTA GGAGTGCATC CAGGTAGTTA GGAGGGAGAG GACAACACAT 60
AGTCTCCTAG GTGCAGGCGG CGGGGGAAGT CCGGTGGACA CCTGTGAAGC TAAGTTCCAG 120
GACCTTCTGG GGGCTGTGGA GAGGAAGGGG ACCTTCTCCA GAGGGGCCGT GTTGATTGAC 180
TCATTCTTCT CTGACTCCTC AGAAGCCAGT TCATTGCAGT AGAGGGGCTG TCCTGCAAGT 240
CATATGCTTC TCCTCCTTGC CTTAACTACA GGAATTCCAA GATGTTTACA CAAACTTCAA 300
GGAGTGAACC AAGTTATTAA AAGAGTAGCA ATTAGGGTGG CCCATCCCAG CAATTTAGTT 360
TCCTGTCTAA GGAAGCATGA AGGGGGAGGG GTTTCCAGGG AGGGGAGAGG GAGGGAGCAT 420
TCTTGTCTCC TGATTGGACC GCCCCAGGAT TTCCATTTCT GAACACAGAC ACAGAAGGAG 480
GGAAGAAAGG TTGCCAGATG CCAGCTCCCA GCTCCCTGGA GGAGTTACTC GCCGCCACAG 540
ATGCTCCAGC AGCTGGTTGG GCCCCTCCTC AAAGTGTCTC TCCTGCTTCC TTCTTTTGGG 600
GGATTCTGGC TCAGCTTTGA AAGCCTTTTG GCATCTTTTG CCTGCCTCCA AAAATTAAGC 660
TGTGTTGGAA GCTGCCTGAT AAATCACTCT TTGCACCGTG GCTGCCATGG GGCTTGCAGA 720
GAGTGGCTGC CTAGTGATTT ACCGCGGCTG TCTGAGAGGG CTTTTCCAAG CAGCCAGCGT 780
AGACCAGGGA GTCATCTCTG GCAAAAGGAG CATTTTGTCT AGCTCAAATG GACACTACAG 840
AGAGGAAGTG GGATTGCTTT GTTCAAAACT TGTTGGTCAT CCATTCCTCA AGCCAGCCGG 900
AATCTCCAAG TTCATTTCTT CCATGCAACT TGAGCTCAAG AAAAGAGGTC CAGAAAAGTG 960
GTTTTTCATG ACAGGCCTGC TGGAGCCTTT CCTAGGGGAA GGAGAACTTT CTGGTTCTGA 1020
ACTGCAGTTA CACAATGCTG GGCAGGCCCT CTGATTTGTG GTCATAGTTT CCCAGAACCC 1080
CAAGGGACCC ATCCAGGAAA ACGCCCATGT CCCCTCGCCT GCGTTGTCAT CTGCTCCCTC 1140
CCAAGGGGAT TTTGTTTCCT TGATTGTGTT CCATAGTGGC TGTTGGAAGT CAGGTGCCCT 1200
GGACGCAGCT TGGACAGGAA CCATGTGGTG TGAGGACCTG AGCCTTGTGC ATACGTGGCT 1260
TTTGCTTCTG GTTCTGGCTT GACAGTGTGA CGAGTTAATT AACCTCTTTC ACCTCTAAAT 1320
CTTCATCTCC ATTATCAGAA 1340
|
